TY - JOUR
T1 - Second malignant neoplasms after treatment of childhood acute lymphoblastic leukemia
AU - Schmiegelow, Kjeld
AU - Levinsen, Mette Frandsen
AU - Attarbaschi, Andishe
AU - Baruchel, Andre
AU - Devidas, Meenakshi
AU - Escherich, Gabriele
AU - Gibson, Brenda
AU - Heydrich, Christiane
AU - Horibe, Keizo
AU - Ishida, Yasushi
AU - Liang, Der Cherng
AU - Locatelli, Franco
AU - Michel, Gérard
AU - Pieters, Rob
AU - Piette, Caroline
AU - Pui, Ching Hon
AU - Raimondi, Susana
AU - Silverman, Lewis
AU - Stanulla, Martin
AU - Stark, Batia
AU - Winick, Naomi
AU - Valsecchi, Maria Grazia
N1 - Funding Information:
Supported by Grant No. IG 5017 from the Associazione Italiana per la Ricerca sul Cancro (M.G.V.); St Anna Kinder-krebsforschung; Deutsche Krebshilfe; Fördergemeinschaft Kinderkrebszen-trum Hamburg; Grants No. CA098543 and U10 CA98413 from the Children’s Oncology Group; Grant No. 5 P01CA068484 from the National Cancer Institute; The European Organisation for Research and Treatment of Cancer Charitable Trust and the Schröder Foundation; Direction Recherche Clinique-Assistance Publique-Hôpitaux de Paris; Centre de Recherche en Oncologie, Hematologie et Pediatrie Association; Israel Cancer Association; Hayim Association for Children with Cancer in Israel; Ministry of Health, Labour and Welfare of Japan; Children’s Cancer Association of Japan; Grant No. R40-A2154 from the Danish Cancer Society; Danish Childhood Cancer Foundation; Swedish Childhood Cancer Foundation; Grant No. CA-21765 from the National Institutes of Health; American Lebanese Syrian Associated Charities; Childhood Cancer Foundation Taiwan; and the Medical Research Council (UK).
Funding Information:
Supported by Grant No. IG 5017 from the Associazione Italiana per la Ricerca sul Cancro (M.G.V.); St Anna Kinder-krebsforschung; Deutsche Krebshilfe; F?rdergemeinschaft Kinderkrebszen-trum Hamburg; Grants No. CA098543 and U10 CA98413 from the Children?s Oncology Group; Grant No. 5 P01CA068484 from the National Cancer Institute; The European Organisation for Research and Treatment of Cancer Charitable Trust and the Schr?der Foundation; Direction Recherche Clinique-Assistance Publique-H?pitaux de Paris; Centre de Recherche en Oncologie, Hematologie et Pediatrie Association; Israel Cancer Association; Hayim Association for Children with Cancer in Israel; Ministry of Health, Labour and Welfare of Japan; Children?s Cancer Association of Japan; Grant No. R40-A2154 from the Danish Cancer Society; Danish Childhood Cancer Foundation; Swedish Childhood Cancer Foundation; Grant No. CA-21765 from the National Institutes of Health; American Lebanese Syrian Associated Charities; Childhood Cancer Foundation Taiwan; and the Medical Research Council (UK). We thank all participating centers, data managers, and local physicians as well as patients and parents. We also thank Hester de Groot, data manager of the Dutch Childhood Oncology Group; Jane O?Brien, Leukemia Program Manager, and Kristen Stevenson, statistician (Dana-Farber Cancer Institute); Yoshifumi Kawano, MD, and Yasuto Shimomura, MD, for data collection (Japanese Pediatric Leukemia/Lymphoma Study Group); and Mats Heyman, Nordic Society of Paediatric Haematology and Oncology leukemia registry manager.
Publisher Copyright:
© 2013 by American Society of Clinical Oncology.
PY - 2013/7/1
Y1 - 2013/7/1
N2 - Purpose: Second malignant neoplasms (SMNs) after diagnosis of childhood acute lymphoblastic leukemia (ALL) are rare events. Patients and Methods: We analyzed data on risk factors and outcomes of 642 children with SMNs occurring after treatment for ALL from 18 collaborative study groups between 1980 and 2007. Results: Acute myeloid leukemia (AML; n 186), myelodysplastic syndrome (MDS; n 69), and nonmeningioma brain tumor (n 116) were the most common types of SMNs and had the poorest outcome (5-year survival rate, 18.1% ± 2.9%, 31.1% ± 6.2%, and 18.3% ± 3.8%, respectively). Five-year survival estimates for AML were 11.2% ± 2.9% for 125 patients diagnosed before 2000 and 34.1% ± 6.3% for 61 patients diagnosed after 2000 (P < .001); 5-year survival estimates for MDS were 17.1% ± 6.4% (n = 36) and 48.2% ± 10.6% (n = 33; P = .005). Allogeneic stem-cell transplantation failed to improve outcome of secondary myeloid malignancies after adjusting for waiting time to transplantation. Five-year survival rates were above 90% for patients with meningioma, Hodgkin lymphoma, thyroid carcinoma, basal cell carcinoma, and parotid gland tumor, and 68.5% ± 6.4% for those with non-Hodgkin lymphoma. Eighty-nine percent of patients with brain tumors had received cranial irradiation. Solid tumors were associated with cyclophosphamide exposure, and myeloid malignancy was associated with topoisomerase II inhibitors and starting doses of methotrexate of at least 25 mg/m2 per week and mercaptopurine of at least 75 mg/m2 per day. Myeloid malignancies with monosomy 7/5q- were associated with high hyperdiploid ALL karyotypes, whereas 11q23/MLL-rearranged AML or MDS was associated with ALL harboring translocations of t(9;22), t(4;11), t(1;19), and t(12;21) (P = .03). Conclusion: SMNs, except for brain tumors, AML, and MDS, have outcomes similar to their primary counterparts.
AB - Purpose: Second malignant neoplasms (SMNs) after diagnosis of childhood acute lymphoblastic leukemia (ALL) are rare events. Patients and Methods: We analyzed data on risk factors and outcomes of 642 children with SMNs occurring after treatment for ALL from 18 collaborative study groups between 1980 and 2007. Results: Acute myeloid leukemia (AML; n 186), myelodysplastic syndrome (MDS; n 69), and nonmeningioma brain tumor (n 116) were the most common types of SMNs and had the poorest outcome (5-year survival rate, 18.1% ± 2.9%, 31.1% ± 6.2%, and 18.3% ± 3.8%, respectively). Five-year survival estimates for AML were 11.2% ± 2.9% for 125 patients diagnosed before 2000 and 34.1% ± 6.3% for 61 patients diagnosed after 2000 (P < .001); 5-year survival estimates for MDS were 17.1% ± 6.4% (n = 36) and 48.2% ± 10.6% (n = 33; P = .005). Allogeneic stem-cell transplantation failed to improve outcome of secondary myeloid malignancies after adjusting for waiting time to transplantation. Five-year survival rates were above 90% for patients with meningioma, Hodgkin lymphoma, thyroid carcinoma, basal cell carcinoma, and parotid gland tumor, and 68.5% ± 6.4% for those with non-Hodgkin lymphoma. Eighty-nine percent of patients with brain tumors had received cranial irradiation. Solid tumors were associated with cyclophosphamide exposure, and myeloid malignancy was associated with topoisomerase II inhibitors and starting doses of methotrexate of at least 25 mg/m2 per week and mercaptopurine of at least 75 mg/m2 per day. Myeloid malignancies with monosomy 7/5q- were associated with high hyperdiploid ALL karyotypes, whereas 11q23/MLL-rearranged AML or MDS was associated with ALL harboring translocations of t(9;22), t(4;11), t(1;19), and t(12;21) (P = .03). Conclusion: SMNs, except for brain tumors, AML, and MDS, have outcomes similar to their primary counterparts.
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U2 - 10.1200/JCO.2012.47.0500
DO - 10.1200/JCO.2012.47.0500
M3 - Article
C2 - 23690411
AN - SCOPUS:84883119415
SN - 0732-183X
VL - 31
SP - 2469
EP - 2476
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 19
ER -